A47.E452 JACC March 9, 2010 Volume 55, issue 10A
HYPERTENSION, LIPIDS AND PREVENTION IMPACT OF LOW DOSE ASPIRIN ON ACETYLCHOLINE-INDUCED CORONARY ARTERY SPASM AND 12 MONTH CLINICAL OUTCOME ACC Oral Contributions Georgia World Congress Center, Room B408 Monday, March 15, 2010, 11:30 a.m.-11:45 a.m.
Session Title: Antiplatelet Agents and Coronary Artery Disease Abstract Category: Pharmacology/Hormones/Lipids—Clinical Presentation Number: 0908-07 Authors: Ji Young Park, Seung Woon Rha, Kanhaiya L. Poddar, Sureshkumar Ramasamy, Lin Wang, Byoung Geol Choi, Ji Bak Kim, Seung Yong Shin, Un Jung Choi, Cheol Ung Choi, Hong Euy Lim, Jin Won Kim, Eung Ju Kim, Chang Gyu Park, Hong Seog Seo, Dong Joo Oh, Korea University Guro Hospital, Seoul, South Korea Background Aspirin is a non-selective COX inhibitor and high dose aspirin can aggravates coronary artery spasm (CAS). However whether low dose aspirin can similarly impact on coronary spasm is largely unknown. We evaluated the impact of low dose asprin on acetylcholine (Ach) induced coronary artery spasm (CAS) and 12 month clinical outcome. Methods A total 1286 consecutive patients without significant coronary artery disease who had taken low dose aspirin (less than 100mg) and underwent the Ach provocation test by injecting incremental doses of 20, 50, 100 ug into between November 2004 and March 2009.The Ach provocation test results and 12 clinical outcomes were compared between the Aspirin group (n=287) and non-aspirin group (n=999). Results The baseline clinical characteristics showed that the classic risk factors including diabetes mellitus (20.6% vs 7.3%, p<0.01), hypertension (59.3% vs 35.9%, p<0.01), hyperlipidemia (21.6% vs 14.9%, p=0.01) and smoking (34.8% vs 28.5%, p=0.04) were more common in the aspirin groups. After Ach injection, the rate of positive provocation test result, chest pain, diffuse and severe CAS pattern were more common in the Aspirin group (Table). Multivariate logistic analysis showed that aspirin itself was an independent risk factor for Ach induced CAS (Adjusted odd ratio; 1.28, 95% confidence interval; 1.01-1.62, p=0.037). 12 month clinical outcomes including death, myocardial infarction (MI) were similiar between two groups. However, repeat spasm test due to recurrent chest pain was more common in aspirin group (2.8% vs 0.2%, p<0.01). Conclusion In our study, low dose aspirin was an independent risk factor of Ach induced significant CAS and associated with diffuse spasm and repeat spasm test due to recurrent chest pain. However,12 month clinical outcome including death and MI was not associated with aspirin. Special caution should be regarding even low dose aspirin prescription in patients who are suspicious of CAS. Table. Acetylcholine provocation test results and 12 Clinical outcomes Variables, n(%)
Aspirin group (n=287)
Non-Aspirin group (n=999)
P value
Ach Provocation (+) Chest pain (+) Provocation to Ach dose A1 (20μg) A2 (50μg) Spasm after Ach injection Diffuse Severe spasm (>70%) Death Myocardial Infarction Spasm FU d/t recurrent chest pain
188 (66.2) 119 (41.5)
545 (55.3) 419 (41.9)
<0.01* 0.05
11 (3.8) 96 (36.0)
38 (3.8) 285 (29.7)
1.00 0.05*
156 (54.4)
456 (45.6)
<0.01*
94 (49.5) 1 (0.3) 1 (0.3) 8 (2.8)
269 (48.8) 1 (0.1) 0 (0.0) 2 (0.2)
<0.01* 0.39 0.23 <0.01*